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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 14 (1981), S. 203-207 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 11 (1978), S. 534-539 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 11 (1978), S. 1298-1298 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of organic chemistry 43 (1978), S. 3526-3530 
    ISSN: 1520-6904
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of organic chemistry 43 (1978), S. 3518-3526 
    ISSN: 1520-6904
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Polymer bulletin 17 (1987), S. 189-195 
    ISSN: 1436-2449
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Summary The new monomer N-methy1-N-butyryldehydroalanine methyl ester was obtained in good yield by N-methylation and base catalyzed ring opening of racemic 2-propy1-4-methoxycarbonyl-2-oxazoline. The oxazoline was prepared in high yield from (R,S)-serine methyl ester hydrochloride and ethyl butyroimidate. Attempted radical and anionic homopolymerization of purified monomer failed. Radical copolymerization with methyl methacrylate was also unsuccessful, although copolymerization with the less hindered methyl acrylate did produce copolymer as determined by high resolution 13C NMR. Unsubstituted N-butyryldehydroalanine methyl ester was prepared by an alternative route and was shown to spontaneously homopolymerize to high polymer. Space-filling models of the monomers indicate steric hindrance for approach of the N-methylated monomer to the active chain end, consistent with difficult homopolymerization.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 25 (1987), S. 161-167 
    ISSN: 0887-6258
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 2241-2247 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: It is clearly demonstrated here that ethyl α-(hydroxymethyl)acrylate (EHMA) is a unique monomer for increasing the dimensional stability and physical properties of balsa wood. Copolymers containing EHMA, and especially EHMA-styrene mixtures, were shown to improve the dimensional stability (water soak test) and the absolute mechanical properties of balsa wood. Improvements in specific modulus and specific toughness (absolute properties divided by specific gravity) were achieved using an EHMA-styrene monomer mixture with polybutadiene diacrylate as cross-linker and toughening agent, with the best results obtained at low (10-40%) weight gain. This is the first report that we are aware of describing specific property improvement greater than expected based on density increase. These improvements in modulus and toughness were ascribed to efficient penetration of monomers into the cell walls. Solid-state NMR and scanning electron microscopy confirmed strong interaction of the copolymers generated in situ with wood cell wall components, consistent with the property improvements obtained. The combination of a light-weight, renewable wood precursor with synergistic reinforcement by this combination of monomers offers unique opportunities for increased use of wood-polymer composites in a wide variety of structural and insulating applications. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 370-375 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Ethyl α-hydroxymethyl acrylate (EHMA) was synthesized and evaluated as a candidate for wood impregnation and in-situ polymerization. Southern Pine softwood was impregnated under a variety of conditions with EHMA alone and with various comonomers plus free radical initiator. Following thermal polymerization, the wood-polymer composites were tested for increased dimensional stability (water soaking swell resistance) and mechanical properties over untreated wood. The greatest increase in dimensional stability was attained using EHMA alone, while the maximum compression modulus was achieved by impregnating with 1:1 EHMA-styrene and styrene alone. The composites were further characterized by 13C CP/MAS solid state NMR and scanning electron microscopy.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 2225-2239 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: New and reliable test methods have been developed, and are under development, for the physical characterization of wood and whole wood-polymer composites (WPC is used in this article to refer to polymer-impregnated whole wood). The methods described here have been designed for smaller samples than are required for most ASTM tests. It should be stressed that, when comparing treated samples to untreated samples in any type of testing, the initial density or specific gravity (density before treatment) of the treated sample should be the same as the untreated control sample. If possible, measurements should be made on a given sample before and after treatment; on a split sample, half should be treated and compared with the untreated half. If there is much variation in density between samples within a group, the effectiveness of the treatment cannot be determined with an acceptable degree of accuracy, since whole wood varies greatly between specimens and density is a major factor contributing to property variability. For example, swelling (due to moisture uptake), modulus, toughness, surface hardness, and compressive strength of wood all increase dramatically with increasing density for both untreated whole wood and WPCs.Scanning electron microscopy, coupled with x-ray energy analysis, indicated the presence or absence of good interaction between wood components and in situ formed polymer. For example, poly(EHMA) (the homopolymer of ethyl α-hydroxymethylacrylate) and wood components were seen to be strongly bonded, and x-ray activation elemental analysis confirmed the presence of poly(EHMA) and its copolymers within the wood cell walls. On the other hand, proton spin-lattice relaxation in the rotating frame (T1p) measurements (by 13C solid-state NMR) for balsa / EHMA WPCs gave two separate sets of relaxation times, one each for unique peaks corresponding to either the polymer or the wood components. It is probable that the region of interaction between poly(EHMA) and the wood component in the balsa / EHMA WPC (the interphase region) is small, as compared to the individual components, and is not observed. This result is consistent with a two-parameter relaxation process for the peak at ca. 61 ppm, which includes overlapping peaks for the hydroxymethyl carbons of poly(EHMA) and cellulose. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
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